Speciation of reactive sulfur species and their reactions with alkylating agents: do we have any clue about what is present inside the cell?

被引:90
作者
Bogdandi, Virag [1 ]
Ida, Tomoaki [2 ]
Sutton, Thomas R. [3 ]
Bianco, Christopher [4 ]
Ditroi, Tamas [1 ]
Koster, Grielof [3 ]
Henthorn, Hillary A. [5 ]
Minnion, Magda [3 ]
Toscano, John P. [4 ]
van der Vliet, Albert [6 ]
Pluth, Michael D. [5 ]
Feelisch, Martin [3 ]
Fukuto, Jon M. [7 ]
Akaike, Takaaki [2 ]
Nagy, Peter [1 ]
机构
[1] Natl Inst Oncol, Dept Mol Immunol & Toxicol, Rath Gyorgy Utca 7-9, H-1122 Budapest, Hungary
[2] Tohoku Univ, Dept Environm Med & Mol Toxicol, Grad Sch Med, Sendai, Miyagi 9808575, Japan
[3] Univ Southampton, Univ Hosp Southampton NHS Fdn Trust, Clin & Expt Sci, Fac Med, Southampton, Hants, England
[4] Johns Hopkins Univ, Dept Chem, Charles & 34Th St, Baltimore, MD 21218 USA
[5] Univ Oregon, Inst Mat Sci, Dept Chem & Biochem, Inst Mol Biol, Eugene, OR 97403 USA
[6] Univ Vermont, Dept Pathol & Lab Med, Robert Larner MD Coll Med, Burlington, VT USA
[7] Sonoma State Univ, Dept Chem, Rohnert Pk, CA 94928 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
HYDROGEN-SULFIDE OXIDATION; MITOCHONDRIAL BIOENERGETIC FUNCTION; POLYSULFIDE IONS; EQUILIBRIUM DISTRIBUTION; AQUEOUS-SOLUTIONS; REDOX CHEMISTRY; H2S; PERSULFIDES; CYSTEINE; ACID;
D O I
10.1111/bph.14394
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
BACKGROUND AND PURPOSE Posttranslational modifications of cysteine residues represent a major aspect of redox biology, and their reliable detection is key in providing mechanistic insights. The metastable character of these modifications and cell lysis-induced artifactual oxidation render current state-of-the-art protocols to rely on alkylation-based stabilization of labile cysteine derivatives before cell/tissue rupture. An untested assumption in these procedures is that for all cysteine derivatives, alkylation rates are faster than their dynamic interchange. However, when the interconversion of cysteine derivatives is not rate limiting, electrophilic labelling is under Curtin-Hammett control; hence, the final alkylated mixture may not represent the speciation that prevailed before alkylation. EXPERIMENTAL APPROACH Buffered aqueous solutions of inorganic, organic, cysteine, GSH and GAPDH polysulfide species were used. Additional experiments in human plasma and serum revealed that monobromobimane can extract sulfide from the endogenous sulfur pool by shifting speciation equilibria, suggesting caution should be exercised when interpreting experimental results using this tool. KEY RESULTS In the majority of cases, the speciation of alkylated polysulfide/thiol derivatives depended on the experimental conditions. Alkylation perturbed sulfur speciation in both a concentration-and time-dependent manner and strong alkylating agents cleaved polysulfur chains. Moreover, the labelling of sulfenic acids with dimedone also affected cysteine speciation, suggesting that part of the endogenous pool of products previously believed to represent sulfenic acid species may represent polysulfides. CONCLUSIONS AND IMPLICATIONS We highlight methodological caveats potentially arising from these pitfalls and conclude that current derivatization strategies often fail to adequately capture physiological speciation of sulfur species.
引用
收藏
页码:646 / 670
页数:25
相关论文
共 78 条
  • [1] Nucleophilic substitution of alkyl halides by electrogenerated polysulfide ions in N,N-dimethylacetamide
    Ahrika, A
    Robert, J
    Anouti, M
    Paris, J
    [J]. ACTA CHEMICA SCANDINAVICA, 1999, 53 (07): : 513 - 520
  • [2] Cysteinyl-tRNA synthetase governs cysteine polysulfidation and mitochondrial bioenergetics
    Akaike, Takaaki
    Ida, Tomoaki
    Wei, Fan-Yan
    Nishida, Motohiro
    Kumagai, Yoshito
    Alam, Md. Morshedul
    Ihara, Hideshi
    Sawa, Tomohiro
    Matsunaga, Tetsuro
    Kasamatsu, Shingo
    Nishimura, Akiyuki
    Morita, Masanobu
    Tomizawa, Kazuhito
    Nishimura, Akira
    Watanabe, Satoshi
    Inaba, Kenji
    Shima, Hiroshi
    Tanuma, Nobuhiro
    Jung, Minkyung
    Fujii, Shigemoto
    Watanabe, Yasuo
    Ohmuraya, Masaki
    Nagy, Peter
    Feelisch, Martin
    Fukuto, Jon M.
    Motohashi, Hozumi
    [J]. NATURE COMMUNICATIONS, 2017, 8
  • [3] Alexander SPH, 2017, BRIT J PHARMACOL, V174, pS272, DOI [10.1111/bph.13877, 10.1111/bph.13882]
  • [4] [Anonymous], J FR HYDROL
  • [5] [Anonymous], ANN CHIM PHYS
  • [6] [Anonymous], ORGANIC SULFUR COMPO
  • [7] [Anonymous], METHODS MOL BIOL
  • [8] The Intersection of NO and H2S: Persulfides Generate NO from Nitrite through Polysulfide Formation
    Bailey, T. Spencer
    Henthorn, Hillary A.
    Pluth, Michael D.
    [J]. INORGANIC CHEMISTRY, 2016, 55 (24) : 12618 - 12625
  • [9] Reactions of isolated persulfides provide insights into the interplay between H2S and persulfide reactivity
    Bailey, T. Spencer
    Pluth, Michael D.
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2015, 89 : 662 - 667
  • [10] The reaction of hydrogen sulfide with disulfides: formation of a stable trisulfide and implications for biological systems
    Bianco, Christopher L.
    Akaike, Takaaki
    Ida, Tomoaki
    Nagy, Peter
    Bogdandi, Virag
    Toscano, John P.
    Kumagai, Yoshito
    Henderson, Catherine F.
    Goddu, Robert N.
    Lin, Joseph
    Fukuto, Jon M.
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 2019, 176 (04) : 671 - 683